Linked Data
MyVariant Identifiers:
chr10:g.112335107T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110575349T>A , CM000672.2:g.110575349T>A | GRCh38 |
| NC_000010.10:g.112335107T>A , CM000672.1:g.112335107T>A | GRCh37 |
| NC_000010.9:g.112325097T>A | NCBI36 |
| NG_012217.1:g.12659T>A , LRG_774:g.12659T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.277T>A | ||
| ENST00000687823.1:n.58T>A | ||
| ENST00000689932.1:n.2207T>A | ||
| ENST00000691297.1:n.277T>A | ||
| ENST00000691527.1:n.234T>A | ||
| ENST00000692792.1:n.263T>A | ||
| ENST00000361804.5:c.144T>A MANE Select | ENSP00000354720.5:p.Val48= | |
| ENST00000361804.4:c.144T>A | ENSP00000354720.4:p.Val48= | |
| ENST00000462899.1:n.290T>A | ||
| NM_005445.3:c.144T>A , LRG_774t1:c.144T>A | NP_005436.1:p.Val48= | |
| NM_005445.4:c.144T>A MANE Select | NP_005436.1:p.Val48= |